Schneider E, Fischer P A
Dtsch Med Wochenschr. 1982 Feb 5;107(5):175-9. doi: 10.1055/s-2008-1069894.
Forty patients with severe Parkinson's disease (23 men, 17 women) who had been treated for six years with L-dopa-decarboxylase inhibitor, were part of a placebo-controlled double-blind trial to test the effectiveness of bromocriptin. In all patients the effectiveness of L-dopa had been decreasing, 34 patients had L-dopa-induced dyskinesias, 35 "on-off" symptoms. Bromocriptin dosage was gradually increased to a total dose of 30 - 40 mg daily. This led to a 25% reduction in L-dopa requirements. The symptoms of Parkinson's disease were favourably influenced, with rigor, tremor and also walking disturbances responding better than bradykinesia of the hands. At the same time, there was a marked prolongation of the periods of good mobility ("on" time) from 7 to 10.8 hours without influence on other "on-off" symptoms such as paradoxical akinesia. Two patients had to be excluded from the trial because the treatment caused side effects (orthostatic hypotension, exogenous psychotic symptoms). Other side effects, such as nausea and mild forms of collapse, could be controlled by drugs.
40例重度帕金森病患者(23例男性,17例女性),使用左旋多巴脱羧酶抑制剂治疗6年,参与了一项安慰剂对照双盲试验,以测试溴隐亭的疗效。所有患者左旋多巴的疗效均在下降,34例患者出现左旋多巴诱发的运动障碍,35例有“开-关”症状。溴隐亭剂量逐渐增加至每日总剂量30 - 40毫克。这使得左旋多巴的需求量减少了25%。帕金森病的症状得到了有利影响,僵直、震颤以及行走障碍的改善比手部运动迟缓更好。同时,良好运动状态(“开”期)的时长显著延长,从7小时延长至10.8小时,且对其他“开-关”症状如反常运动不能没有影响。两名患者因治疗引起副作用(体位性低血压、外源性精神症状)而不得不退出试验。其他副作用,如恶心和轻度虚脱,可用药物控制。